GlyCosmos Portal

Source	Last Updated
GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
GlyGen	June 4, 2024
The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **2076 - 2100** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism ▲	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q15800	Methylsterol monooxygenase 1	MSMO1 DESP4 ERG25 SC4MOL	Homo sapiens (human)	2	1	Laron syndrome achondroplasia actinic keratosis blepharitis cancer diabetes mellitus embryoma ichthyosis idiopathic scoliosis microcephaly obesity parapsoriasis psoriasis pustulosis of palm and sole seborrheic keratosis skin disease type 2 diabetes mellitus
A0A0A0MSX4	Roundabout guidance receptor 1	ROBO1	Homo sapiens (human)	2	0
Q8TC56	Golgi-associated RAB2 interactor protein 3	GARIN3 FAM71B	Homo sapiens (human)	4	2
A0A3B3IRL1	LMBR1 domain containing 1 (Fragment)	LMBRD1	Homo sapiens (human)	1	0
Q86XE5	4-hydroxy-2-oxoglutarate aldolase, mitochondrial	HOGA1 C10orf65 DHDPSL	Homo sapiens (human)	3	1	calcinosis calcium metabolism disease cholestasis chronic kidney disease hypercalcemia nephrocalcinosis nephrolithiasis phosphorus metabolism disease primary hyperoxaluria
A0A0K0KRA1	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
D6MKT2	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
O95427	GPI ethanolamine phosphate transferase 1	PIGN MCD4	Homo sapiens (human)	4	8	Dandy-Walker syndrome Hirschsprung's disease Marfan syndrome Meckel syndrome Miller-Dieker lissencephaly syndrome Paget's disease of bone acute monocytic leukemia acute myeloid leukemia amblyopia atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect autosomal dominant polycystic kidney disease basal ganglia disease blepharitis blepharospasm cerebral degeneration chromosome 17p13.1 deletion syndrome chronic recurrent multifocal osteomyelitis cleft palate colorectal cancer colorectal carcinoma congenital diaphragmatic hernia congenital nystagmus cryptorchidism dissociated nystagmus duodenal atresia epilepsy esophagitis esotropia essential thrombocythemia focal hand dystonia gastroesophageal reflux disease gingival hypertrophy gingival overgrowth heart septal defect holoprosencephaly 1 holoprosencephaly hydrocephalus hydronephrosis hypospadias idiopathic interstitial pneumonia imperforate anus intellectual disability isolated cleft palate large intestine cancer learning disability lingual-facial-buccal dyskinesia lissencephaly lung adenocarcinoma lung cancer mammary Paget's disease microphthalmia monocular esotropia movement disease multiple congenital anomalies-hypotonia-seizures syndrome 1 myelodysplastic syndrome omphalocele patent ductus arteriosus patent foramen ovale pathologic nystagmus peptic esophagitis polyhydramnios postinflammatory pulmonary fibrosis primary pulmonary hypertension pulmonary fibrosis recurrent corneal erosion renal agenesis situs inversus spontaneous ocular nystagmus strabismic amblyopia tetralogy of Fallot tuberous sclerosis umbilical hernia vesicoureteral reflux visual epilepsy
C6JSY2	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q9HCE3	Zinc finger protein 532	ZNF532 KIAA1629	Homo sapiens (human)	4	1
A0A141AZC8	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
L0HNE1	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q9NRG0	Chromatin accessibility complex protein 1	CHRAC1 CHRAC15	Homo sapiens (human)	0	1
Q9BS26	Endoplasmic reticulum resident protein 44	ERP44 KIAA0573 TXNDC4	Homo sapiens (human)	9	6
P31274	Homeobox protein Hox-C9	HOXC9 HOX3B	Homo sapiens (human)	3	1
E5D6M4	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q9GZR1	Sentrin-specific protease 6	SENP6 KIAA0797 SSP1 SUSP1	Homo sapiens (human)	2	2
A0A0A7C4Q3	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
B2YG92	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
A0A076V826	Rhodopsin	RHO	Homo sapiens (human)	2	0
P46721	Solute carrier organic anion transporter family member 1A2	SLCO1A2 OATP OATP1 OATP1A2 SLC21A3	Homo sapiens (human)	5	0
Q92765	Secreted frizzled-related protein 3	FRZB FIZ FRE FRP FRZB1 SFRP3	Homo sapiens (human)	1	11
Q6F5E8	Capping protein, Arp2/3 and myosin-I linker protein 2	CARMIL2 LRRC16C RLTPR	Homo sapiens (human)	2	2
P51843	Nuclear receptor subfamily 0 group B member 1	NR0B1 AHC DAX1	Homo sapiens (human)	1	2
Q9GZX6	Interleukin-22	IL22 ILTIF ZCYTO18	Homo sapiens (human)	3	0

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